NM_007294.4:c.1703C>T

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HGVS Expressions

  • NG_005905.2:g.124156C>T
  • NM_007294.4:c.1703C>T
  • NP_009225.1:p.Pro568Leu
  • NC_000017.11:g.43093828G>A

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

80356910

Clinvar

54329

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.72LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage II lobular carcinoma
114480.73LebanonUncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage IV ductal carcinoma
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Contributors

  • Asha Deepthi: 13.01.2021

Edit History

  • Asha Deepthi: 13.01.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.